gudid Primary ID: N/A

ST AIA-PACK LH II (UDI N/A)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The ST AIA-PACK LH II (Model/Catalog Number: N/A) is a medical device manufactured by TOSOH CORPORATION. This product is indexed under FDA Product Code / Category Classification CEP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: N/A
Product Code / EMDN: CEP
Device Name
Database Sync Date: 2026-08-09 09:29:19

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of ST AIA-PACK LH II?

The registered manufacturer of record for ST AIA-PACK LH II is TOSOH CORPORATION.

What is the Primary UDI-DI identifier for ST AIA-PACK LH II?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is N/A.

What classification code is assigned to this device?

This device is registered under product classification code CEP.

Similar Classification Devices (CEP)

Other Devices by TOSOH CORPORATION

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